| Literature DB >> 11044947 |
S Ziyeh1, R Berger, K Reisner.
Abstract
Osteogenesis imperfecta (OI) is an inherited generalized disorder of type-I collagen synthesis often associated with hearing loss. We present a case of OI type I in which hearing loss led to examination of the temporal bone with MRI. In the osseous otic capsule MRI demonstrated pericochlear lesions with soft tissue signal intensity and contrast enhancement. Changes similar to otosclerosis have been described in the temporal bone of OI patients when applying CT, but reports on MRI findings do not yet exist.Entities:
Mesh:
Year: 2000 PMID: 11044947 DOI: 10.1007/s003300000429
Source DB: PubMed Journal: Eur Radiol ISSN: 0938-7994 Impact factor: 5.315